Sulfur 8 Scalp Therapy Medicated Dandruff Control
Sulfur 8 Scalp Therapy Medicated Dandruff Control is an FDA drug label for the active ingredient SALICYLIC ACID manufactured by J. Strickland and Co. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231021.
Generic: SALICYLIC ACID
Manufacturer: J. Strickland and Co.
Product Type: HUMAN OTC DRUG
Route: TOPICAL
Dosage Form:
NDC: 12022-032
Application: M032
Effective: 20231021
Active Ingredients: Active Ingredient Salicylic Acid, 2% Purpose Antidandruff
Indications & Usage
Use: Controls scalp itching and flaking due to dandruff
Dosage & Administration
Directions Spray to apply to the affected area 1-4 times daily, or as directed by a doctor
Contraindications
Not available.
Warnings
Warnings For external use only When using this product avoid contact with eyes. If contact, rinse eyes thoroughly with water. Stop use and consult a doctor if condition worsens or does not improve after regular use of this product as directed. Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center at once.
Adverse Reactions
Not available.
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